Clinical Research Associate Regional Monitoring
hace 4 semanas
Job Overview
We are seeking a skilled Clinical Research Associate to join our team in Barcelona. As a Regional Monitoring Specialist, you will be responsible for monitoring clinical studies in phases II-III, ensuring adherence to Good Clinical Practices and investigator integrity.
Key Responsibilities
- Monitoring clinical studies in phases II-III
- Assuring adherence to Good Clinical Practices and investigator integrity
- Identification, qualification, and initiation of investigators and their sites
- Supervising study conduct according to GCP requirements and all applicable laws
Requirements
- Bachelor degree in life-science
- Min 1 year monitoring experience as CRA within a CRO, Pharma, Biotech in Netherlands
- Experience in commercial studies
- Experience with site initiation, site close out
- Experience in clinical studies phase II-III
- Fluent English & Spanish
- Excellent communication skills
- A full clean drivers license
About Us
Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access.
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